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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1958569생성일: 2026년 10월 27일

Water → 4-Chloro-2-amino-6-[1-(2-trifluoromethylphenyl)-2,2,2-trifluoro-ethoxy]-pyrimidine

https://huagongshe.com/reaction/1958569

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물2-Amino-4,6-dichloropyrimidineHCID 65522—
반응물2,2,2-Trifluoro-1-[2-(trifluoromethyl)phenyl]ethan-1-olHCID 61644993—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물4-Chloro-2-amino-6-[1-(2-trifluoromethylphenyl)-2,2,2-trifluoro-ethoxy]-pyrimidineHCID 8661429371.8%

반응 조건

온도70 °C

반응 단계

NaH (80 mg, 60%, 3.0 mmol) was added to a solution of 1-(2-trifluoromethylphenyl)-2,2,2-trifluoro-ethanol (244 mg, 1 mmol) in 10 ml of anhydrous THF. The mixture was stirred for 20 minutes, 2-amino-4,6-dichloro-pyrimidine (164 mg, 1 mmol) was added and then the reaction mixture was heated at 70° C. for 1 hour. After cooling, 5 ml water was added and ethyl acetate (20 ml) was used to extract the product. The organic layer was dried over sodium sulfate. The solvent was removed by rotovap to give 267 mg of 4-chloro-6-[2,2,2-trifluoro-1-(2-trifluoromethylphenyl)-ethoxy]-pyrimidin-2-ylamine, yield 71%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08410121B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-d905cee97e3d40ac83ec4bbbee372963
출처 메모uspto-grants-2013_04